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BioWorld - Friday, April 10, 2026
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FDA clears design of phase III oritavancin trials SOLO-1 and -2
Dec. 1, 2010
New Juvista formulation for children significantly improves scar appearance
Nov. 23, 2010
CIS Bio withdraws E.U. marketing authorization for NeoSpect
Nov. 23, 2010
EMA's COMP recommends orphan status for paquinimod in systemic sclerosis
Nov. 18, 2010
EMA accepts Pixuvri MAA for non-Hodgkin's lymphoma for review
Nov. 18, 2010
Roche reports on third quarter of 2010
Nov. 18, 2010
EMA approves Cell Therapeutics' pediatric investigation plan for Pixuvri
Nov. 17, 2010
EMA orphan drug status for SBC-102 in LAL deficiency / News in Context
Nov. 17, 2010
EMA committee recommends orphan drug status for ThermoDox in primary liver cancer
Nov. 12, 2010
Schering-Plough Europe withdraws MAA for Zenhale
Nov. 11, 2010
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